Autosomal recessive nonsyndromic hearing loss 59

Synonyms: DFNB59 Nonsyndromic Hearing Loss and Deafness; Deafness, autosomal recessive 59

Summary

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the PJVK gene. [from MONDO]

Available tests

15 tests are in the database for this condition.

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Clinical tests (15 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

PJVK
36 tests
Also known as: DFNB59, PJVK
Summary: pejvakin

Imported from Human Phenotype Ontology (HPO)

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Ear malformation
- Sensorineural hearing loss disorder
  Sensorineural hearing loss disorder
  - MedGen UID: 9164
  - Concept ID: C0018784
  - Finding: Disease or Syndrome
  Ear malformation
  See: Feature record | Search on this feature

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